Label: PURE FORCE- benzalkonium chloride liquid

  • NDC Code(s): 47593-504-41, 47593-504-59
  • Packager: Ecolab Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated June 30, 2023

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  • Active Ingredient

    Benzalkonium chloride 0.1%

  • Purpose

    Antiseptic handwash

  • Uses

    • for handwashing to decrease bacteria on the skin
    • recommended for repeated use
  • Warnings

    • For external use only

    Do not use

    • In eyes

    When using this product

    • If in eyes, rinse promptly and thoroughly with water
    • discontinue use if irritation and redness develop

    Stop use and ask a doctor if skin irritation or redness occurs for more than 72 hours

    Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • wash hands to remove soil
    • dispense palmful
    • spread to cover hands, rub in well
    • air dry, do not rinse or towel dry
  • Other information

    • for additional information, see Material Safety Data Sheet (MSDS)
    • for emergency medical information in USA, call 1.800.328.0026
  • INACTIVE INGREDIENT

    Inactive ingredients  water (aqua), isopropoyl alcohol, propylene glycol, FDC red 40, FDC blue 1

  • QUESTIONS

    Questions? call 1.866.444.7450

  • Principal Display Panel with Representative Label

    Hand Sanitizing Foam

    Active ingredient:  Benzalkonium chloride 0.1%

    25 FL OZ (750 mL)

    Pure Force™

    Distributed by:                        © 2013 Ecolab USA Inc.

    PureForce                               All Rights Reserved

    370 Wabasha Street North       Made in U.S.A.

    St. Paul, MN 55102                           755509/7100/0713

    representative label

  • INGREDIENTS AND APPEARANCE
    PURE FORCE 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47593-504
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47593-504-41750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/28/2013
    2NDC:47593-504-591250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/28/201309/28/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E10/28/2013
    Labeler - Ecolab Inc. (006154611)
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